RECRUITING

AVAVA MIRIA General Use

Conditions

Acne Acne Scars - Mixed Atrophic and Hypertrophic Scars Wrinkle Pigment; Lesion Skin Texture Disorder

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Study Overview

This clinical trial focuses on testing the efficacy of different digital interventions to promote re-engagement in cancer-related long-term follow-up care for adolescent and young adult (AYA) survivors of childhood cancer.

Description

A general protocol to treat a variety of dermatologic conditions and collect patient feedback. Primary outcome is the collection and analysis of patient questionnaires related to the overall experience of the device treatment. Secondary outcome measures include physician and subject evaluations in regards to improvement seen in the device as well as assessment of side effects.

Official Title

AVAVA MIRIA General Use

Quick Facts

Study Start:2024-09-11

Study Completion:2027-12-30

Study Type:Not specified

Phase:Not Applicable

Enrollment:Not specified

Status:RECRUITING

Study ID

NCT06868615

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Ages Eligible for Study:18 Years to 70 Years

Sexes Eligible for Study:ALL

Accepts Healthy Volunteers:Yes

Standard Ages:ADULT, OLDER_ADULT

Inclusion Criteria	Exclusion Criteria
1. Male or female subjects between 18 to 70 years of age. 2. Dermatologic condition that can be addressed by the laser, including but not limited to: 1. Wrinkles 2. Scars 3. Acne Scars 4. Active Acne 5. Dyschromia 6. Cutaneous Lesions such as Age or Sun Spots 7. Melasma 8. Laxity 3. Willingness to have digital photographs taken of treatment area(s) and agreement with use of photographs for presentation, educational, or marketing purposes. 4. Willingness to comply with the following during the study, including the follow-up period: 1. maintain consistent skin care regimen on treated areas. 2. cover treated areas or have very limited sun exposure and, if requested, use an approved sunscreen of SPF 50 or higher. 3. refrain from using systemic corticosteroids, according to Investigator discretion. 4. refrain from using topical corticosteroids, retinoids, or prescription skin-lightening medications on the treated areas, according to Investigator discretion. 5. refrain from any other procedures in the treatment areas. 5. Willingness and ability to comply with study instructions and return for required visits. 6. Subject has read and signed a written informed consent form. 7. Subject lives within 50 miles of study site. 8. Willingness to shave hair in intended treatment area	1. Skin pathology or condition that could interfere with evaluation of the study procedure, e.g., 2. Systemic treatment prescribed within previous 6 months (e.g., oral medication such as isotretinoin) 3. Surgical treatment in the target areas within previous 6 months (e.g., laser surgery) 4. Active vitiligo, psoriasis, or eczema in the treatment area 5. Injection of dermal filler in the target areas within previous 1 month (e.g., collagen, hyaluronic acid filler) 6. Cosmetic procedures in the target areas within prior 3 months (e.g., laser, microdermabrasion, skin peel) 7. Topical treatment applied to target areas within the previous 1 month or according to Investigator discretion. 8. Active suntan and unable or unlikely to refrain from tanning within the follow-up period. 9. Artificial tanning in the target areas within the previous 1 month (e.g., spray, lotion, tanning bed) or intention to use artificial tanning within the follow-up period. 10. Active localized or systemic infection, or an open wound in area being treated. 11. Lesions in the treatment areas suspicious for malignancy (skin cancer, melanoma) 12. History of abnormal wound healing or abnormal scarring (e.g., hypertrophic or keloid) 13. History of connective tissue disease, such as lupus or scleroderma. 14. Any use of medication that is known to increase sensitivity to light according to Investigator's discretion (e.g., topicals that produce sensitivity to light may be used in areas other than the target area). 15. History of gold therapy. 16. History of disease stimulated by heat, such as recurrent herpes simplex or herpes zoster (shingles) in the treatment area, unless treatment is conducted following a prophylactic regimen. 17. History of radiation to the treatment area or currently undergoing systemic chemotherapy for the treatment of cancer. 18. For Female: Pregnancy or lactation, or intent to become pregnant within the study period. 19. Significant uncontrolled concurrent illness, such as diabetes mellitus or cardiovascular disease, e.g., uncontrolled hypertension. 20. History of immunosuppression/immune deficiency disorder or currently using immunosuppressive medications. 21. Current enrollment in a clinical study of any other unapproved investigational drug or device 22. Any other condition or laboratory value that would, in the professional opinion of the investigator, potentially affect response or participation in this clinical study, or would pose an unacceptable risk to the subject.

Inclusion Criteria

Exclusion Criteria

1. Male or female subjects between 18 to 70 years of age.
2. Dermatologic condition that can be addressed by the laser, including but not limited to:
1. Wrinkles
2. Scars
3. Acne Scars
4. Active Acne
5. Dyschromia
6. Cutaneous Lesions such as Age or Sun Spots
7. Melasma
8. Laxity
3. Willingness to have digital photographs taken of treatment area(s) and agreement with use of photographs for presentation, educational, or marketing purposes.
4. Willingness to comply with the following during the study, including the follow-up period:
1. maintain consistent skin care regimen on treated areas.
2. cover treated areas or have very limited sun exposure and, if requested, use an approved sunscreen of SPF 50 or higher.
3. refrain from using systemic corticosteroids, according to Investigator discretion.
4. refrain from using topical corticosteroids, retinoids, or prescription skin-lightening medications on the treated areas, according to Investigator discretion.
5. refrain from any other procedures in the treatment areas.
5. Willingness and ability to comply with study instructions and return for required visits.
6. Subject has read and signed a written informed consent form.
7. Subject lives within 50 miles of study site.
8. Willingness to shave hair in intended treatment area

1. Skin pathology or condition that could interfere with evaluation of the study procedure, e.g.,
2. Systemic treatment prescribed within previous 6 months (e.g., oral medication such as isotretinoin)
3. Surgical treatment in the target areas within previous 6 months (e.g., laser surgery)
4. Active vitiligo, psoriasis, or eczema in the treatment area
5. Injection of dermal filler in the target areas within previous 1 month (e.g., collagen, hyaluronic acid filler)
6. Cosmetic procedures in the target areas within prior 3 months (e.g., laser, microdermabrasion, skin peel)
7. Topical treatment applied to target areas within the previous 1 month or according to Investigator discretion.
8. Active suntan and unable or unlikely to refrain from tanning within the follow-up period.
9. Artificial tanning in the target areas within the previous 1 month (e.g., spray, lotion, tanning bed) or intention to use artificial tanning within the follow-up period.
10. Active localized or systemic infection, or an open wound in area being treated.
11. Lesions in the treatment areas suspicious for malignancy (skin cancer, melanoma)
12. History of abnormal wound healing or abnormal scarring (e.g., hypertrophic or keloid)
13. History of connective tissue disease, such as lupus or scleroderma.
14. Any use of medication that is known to increase sensitivity to light according to Investigator's discretion (e.g., topicals that produce sensitivity to light may be used in areas other than the target area).
15. History of gold therapy.
16. History of disease stimulated by heat, such as recurrent herpes simplex or herpes zoster (shingles) in the treatment area, unless treatment is conducted following a prophylactic regimen.
17. History of radiation to the treatment area or currently undergoing systemic chemotherapy for the treatment of cancer.
18. For Female: Pregnancy or lactation, or intent to become pregnant within the study period.
19. Significant uncontrolled concurrent illness, such as diabetes mellitus or cardiovascular disease, e.g., uncontrolled hypertension.
20. History of immunosuppression/immune deficiency disorder or currently using immunosuppressive medications.
21. Current enrollment in a clinical study of any other unapproved investigational drug or device
22. Any other condition or laboratory value that would, in the professional opinion of the investigator, potentially affect response or participation in this clinical study, or would pose an unacceptable risk to the subject.

Contacts and Locations

Study Contact

Alexander Denis

CONTACT

6176936669

studies@avavaskin.com

Study Locations (Sites)

AVAVA, Inc.

Waltham, Massachusetts, 02451

United States

Collaborators and Investigators

Sponsor: AVAVA, Inc.

Study Record Dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Registration Dates

Study Start Date2024-09-11

Study Completion Date2027-12-30

Study Record Updates

Study Start Date2024-09-11

Study Completion Date2027-12-30

Terms related to this study

Additional Relevant MeSH Terms

Acne
Acne Scars - Mixed Atrophic and Hypertrophic
Scars
Wrinkle
Pigment; Lesion
Skin Texture Disorder